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One cat with low thyroid hormone had growth issues, and another with high thyroid hormone had skin problems; both got better with treatment.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Blood vessels and specific genes help turn cartilage into bone when bones heal.

Chemotherapy in the first trimester of pregnancy is risky, but in the second and third trimesters, it's generally safe with careful drug selection and timing.

Pannexin 3 is important for bone formation and the development of bone cells.

Caspases are enzymes important for both cell death and various non-lethal cell functions, affecting head development and hair growth, with different caspases playing specific roles.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Adult hair follicle cells can create new hair follicles from corneal cells with the right support.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

A young Saudi girl with uncontrolled type 1 diabetes and hypothyroidism had two rare conditions, Mauriac syndrome and Van Wyk–Grumbach syndrome.

A gene called BMAL1 plays a role in controlling hair growth.

Ezh2 controls skin development by balancing signals for dermal and epidermal growth.

The supplement highlighted advancements and challenges in plastic and reconstructive surgery, including the impact of smoking, chemotherapy, and new treatments like Tafluprost for hair loss.

NSAIDs may not affect soft tissue healing but should be used carefully for bone fractures and more research is needed to understand sex differences in response.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

A child with a rare vitamin D-resistant condition improved with treatment.

Survivors of Stevens-Johnson syndrome/toxic epidermal necrolysis need ongoing care for various long-term health problems.

CD201+ fascia progenitors are essential for wound healing and could be targeted for treating skin conditions.

A 14-year-old girl with no menstrual period was diagnosed with Swyer Syndrome and treated for a related cancer risk.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

Estrogens significantly influence hair growth by interacting with receptors in hair follicles and may help regulate the hair growth cycle.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

The Wnt/β-catenin pathway is important for tissue development and has potential in regenerative medicine, but requires more research for therapeutic use.

Mammals might fail to regenerate not because they lack the right cells, but because of how cells respond to their surroundings, and changing this environment could enhance regeneration.

EVAL membranes help create cell structures that can regrow hair follicles.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

BMP2 needs periosteal tissue to help regenerate mouse middle finger bones within a specific time.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.